Yantao Cai, Wanting Bao, Beili Zhang, A Lucarelli, M Martins, J Guedes, G Huang, M Liang, H Liu, J Huang, P Li, C Wang, X Pang, R Li, D Shi, X Pan, C Ma, G Zhang, J Liao, G Dong, W Zhu, B Wulaer, H Mizoguchi, M Sawahata, S Ubeysinghe, D Kankanamge, W Thotamune, D Wijayaratna, T Mohan, A Karunarathne, Y Liao, J Zeng, J Zhou, G Yang, K Ding, X Zhang, X Wang, L Zhang, Wang Wang, Y Chen, Y Xie, R, H Zhao, J Yin, X Chen, J Wu, W Wang, L Tang, Z Lin, D Li, W Cheng, J Wu, K Wang, Y Hu, W Wei, H Chen, S Liu, F Derakhshan, J Reis-Filho, Y Jiang, D Ma, C Suo, J Shi, M Xue, X Hu, Q Guo, D Li, X Luo, Y Yuan, T Li, H Liu, B Peng, J Ortega, L Gu, Z Chang, G Li, R Nusse, H Clevers, M Nalli, D Masci, A Urbani, La Regina, G Silvestri, R, S Shang, F Hua, Z Hu, Y Li, Jin Van Pelt, G Van Dam, H Yu, X Mesker, W
{"title":"RTKN2, a potential target of breast cancer (BCa), can promote the growth and migration of breast cancer cells","authors":"Yantao Cai, Wanting Bao, Beili Zhang, A Lucarelli, M Martins, J Guedes, G Huang, M Liang, H Liu, J Huang, P Li, C Wang, X Pang, R Li, D Shi, X Pan, C Ma, G Zhang, J Liao, G Dong, W Zhu, B Wulaer, H Mizoguchi, M Sawahata, S Ubeysinghe, D Kankanamge, W Thotamune, D Wijayaratna, T Mohan, A Karunarathne, Y Liao, J Zeng, J Zhou, G Yang, K Ding, X Zhang, X Wang, L Zhang, Wang Wang, Y Chen, Y Xie, R, H Zhao, J Yin, X Chen, J Wu, W Wang, L Tang, Z Lin, D Li, W Cheng, J Wu, K Wang, Y Hu, W Wei, H Chen, S Liu, F Derakhshan, J Reis-Filho, Y Jiang, D Ma, C Suo, J Shi, M Xue, X Hu, Q Guo, D Li, X Luo, Y Yuan, T Li, H Liu, B Peng, J Ortega, L Gu, Z Chang, G Li, R Nusse, H Clevers, M Nalli, D Masci, A Urbani, La Regina, G Silvestri, R, S Shang, F Hua, Z Hu, Y Li, Jin Van Pelt, G Van Dam, H Yu, X Mesker, W","doi":"10.22514/ejgo.2023.108","DOIUrl":null,"url":null,"abstract":"Breast cancer (BCa) is a type of malignancy; however, the exact mechanisms responsible for breast cancer have yet to be elucidated. Rhotekin 2 (RTKN2) is a member of the Rhotekin family. Previous studies demonstrated that RTKN2 is highly expressed in numerous tumors. Previous analysis of the The cancer genome altas (TCGA) database demonstrated that PRKN2 was overexpressed in BCa. However, RTKN2 is rarely reported in BCa and the mechanisms remain unclear. The aim of this study was to elucidate the effect of RTKN2 on the growth of breast cancer cells and investigate the mechanisms involved. Our analysis revealed high expression of RTKN2 in human BCa. The depletion of RTKN2 suppressed the growth of breast cancer cells. In addition, the knockout of RTKN2 restrained the progression of BCa. We also revealed that the knockdown of RTKN2 stimulated cell cycle arrest in BCa. Mechanistically, RTKN2 mediated the Wnt/β-catenin axis to affect the progression of breast cancer. In conclusion, RTKN2 promotes the growth and migration of breast cancer cells by mediating the Wnt/β-catenin axis.","PeriodicalId":11903,"journal":{"name":"European journal of gynaecological oncology","volume":"44 6","pages":"136-136"},"PeriodicalIF":0.5000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://oss.ejgo.net/files/article/20231215-127/pdf/EJGO2023083102.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European journal of gynaecological oncology","FirstCategoryId":"0","ListUrlMain":"https://doi.org/10.22514/ejgo.2023.108","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"OBSTETRICS & GYNECOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Breast cancer (BCa) is a type of malignancy; however, the exact mechanisms responsible for breast cancer have yet to be elucidated. Rhotekin 2 (RTKN2) is a member of the Rhotekin family. Previous studies demonstrated that RTKN2 is highly expressed in numerous tumors. Previous analysis of the The cancer genome altas (TCGA) database demonstrated that PRKN2 was overexpressed in BCa. However, RTKN2 is rarely reported in BCa and the mechanisms remain unclear. The aim of this study was to elucidate the effect of RTKN2 on the growth of breast cancer cells and investigate the mechanisms involved. Our analysis revealed high expression of RTKN2 in human BCa. The depletion of RTKN2 suppressed the growth of breast cancer cells. In addition, the knockout of RTKN2 restrained the progression of BCa. We also revealed that the knockdown of RTKN2 stimulated cell cycle arrest in BCa. Mechanistically, RTKN2 mediated the Wnt/β-catenin axis to affect the progression of breast cancer. In conclusion, RTKN2 promotes the growth and migration of breast cancer cells by mediating the Wnt/β-catenin axis.
期刊介绍:
EJGO is dedicated to publishing editorial articles in the Distinguished Expert Series and original research papers, case reports, letters to the Editor, book reviews, and newsletters. The Journal was founded in 1980 the second gynaecologic oncology hyperspecialization Journal in the world. Its aim is the diffusion of scientific, clinical and practical progress, and knowledge in female neoplastic diseases in an interdisciplinary approach among gynaecologists, oncologists, radiotherapists, surgeons, chemotherapists, pathologists, epidemiologists, and so on.